ClinVar Miner

Submissions for variant GRCh37/hg19 1q24.2(chr1:168439652-168712431)x1

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Cytogenetics and Genomic Microarray,ARUP Laboratories RCV000447824 SCV000502147 uncertain significance See cases no assertion criteria provided clinical testing
ISCA site 1 RCV000512486 SCV000585285 likely benign See cases 2015-06-22 no assertion criteria provided clinical testing

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